| Tag | Content |
|---|
EnhancerAtlas ID | HS180-50998 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chrX:46988360-46989640 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chrX:46988570-46988581 | GCCCCGCCCCC | + | 6.02 | | KLF5 | MA0599.1 | chrX:46988570-46988580 | GCCCCGCCCC | + | 6.02 | | RREB1 | MA0073.1 | chrX:46989259-46989279 | CCCCCCCCCACCCCCCCGGA | + | 6.28 | | SP2 | MA0516.2 | chrX:46988720-46988737 | TCAATCCCCGCCCCCTT | + | 6.48 | | ZNF740 | MA0753.2 | chrX:46989257-46989270 | GCCCCCCCCCCAC | + | 6.29 | | ZNF740 | MA0753.2 | chrX:46989255-46989268 | CCGCCCCCCCCCC | + | 6.64 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chrX | 46988600 | 46988657 | | chrX | 46988400 | 46988600 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH0XI047128 | chrX | 46988000 | 46989999 |
|
Enhancer Sequence | ATCGCTGGAA CCCGGGAGGC GGAGGTTGCA GTGAGCGGAG ATCGTGCCAC TGCACTCCAG 60
CCTGGGCGAC AGAGCTAGAT TCCGTCTCAA AAAAATAAAA AATATAAAAT AAAAAACAGA 120
TAAGCGGGTA GGGAGCTACC GGTGGAACTG AGTTTCCTCT TTAAGGGAAA CGAGGACAAG 180
GACAAGATCC CGTCTTTTCT GCACTCAGTC GCCCCGCCCC CAACGCAAGT AGGCATGTTT 240
ATTGGATGAT AAGAGGGTCA GTCAAAGTAA GGACCAACCC TCTACTGCCA AAAGACACAT 300
ACTACTCAAG GGCCCCTGAC TCAGACGTTC TCACTGGTCG GAAATGCCAT CAATCAAGTT 360
TCAATCCCCG CCCCCTTCTC GCGGAAGAAC TATGGGTGCT AACCTCTCTC TCAGGCCTGC 420
TGTCAATCGG CTCCGCATCC TCTAGTTCTG CACATCCCCG GCCATCAGAG CACGAACTTC 480
TGGTCGGTCC GCCTGCCGTT CTTTCACCTA TAGAGCCCAC CCTCTAAAGG TGTCCAAGCT 540
GCTCCAAAGA ACAATTGATT AACCCAACGG CTGTCTTTGG CCCTCAGAAC TGTCACACCT 600
GGCTCCGCCT CTTCCCGGAC ATCATCTGTT GCACCAGAGA CTGGCGGGTC TGGAAAGAAG 660
CTCTGAGCCC ATCCGCGTTT CTCTGTTGGA CCCTGTCAGG TCTCTTGTTC CGTGTCCAAT 720
GTCAGTCGGG TAGGGAGGCA GTGGGGCAGT CTTGGTTCTC ATCCCACCCC GGAGTCTCTG 780
CGCAGCCACA ATTCAGGAAA ACAATCTGGA GGCGGGTTCA AAACACTAAG ATTGATTGAA 840
CGCGCTGATG GTTTGGTTTT CTCCTATAGC GCTTTGGTAG TGGCTTTTAT CCAGACCGCC 900
CCCCCCCCAC CCCCCCGGAA TGAACCCTGG TATAGAAATG TTACCCGTAT GTGTGCATAT 960
GATTGTTTTT AATATATTTC AATTTGATGA ATCAGCCTTT TTCAAGGTCA GATTCCAGAC 1020
CGACCCTTCT GGCGCCCACC CCCCGCTTTT TTTTTTTTTT TTTTTTTTCC AAAATGAAAG 1080
CTTTCCCAAA GAGGCCACGT TTGTAGGGCT AGTGGAATTT TTTGGAAAAG GGAGAAAGCG 1140
GATTCTGGAT GAGGACAATG GTGGCCCAGA AGTCGCTATG ACTTAAGAGT CTTGGCAGAG 1200
GCAGAGGCTG GGGAAAGCGA GCAGTGTTTT TCATTTAGGT GGCATCTGTA CGAATCCTAG 1260
TTTGGAAAGG TGCGAAGGTT 1280
|
